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- W2359954068 abstract "Three fluorescent indocyanines containing p-carboxybenzyl groups on N atoms in the heterocyclic tings were synthesized under supersonic.The maxima wavelength of the absorption and emission of the dyes were 550-800 nm in water.Compared with those in aqueous solutions,the fluorescence intensity of the dyes in theα/β-cyclodextrin,Al~(3+),Zn~(2+),Sn~(2+)or theα/β-cyclodextrin in the aqueous solutions of the cations became stronger.The crystal shapes of the dyes and their cyclodexttin inclusions were mostly acicular or polygon.The NHS-carboxyl squarylium indocyanine was prepared and used to conjugate with taurine or benzylamine, the results indicated that the dyes could couple covalently to biomass containing free NH_2 group.Structure and some thermal parameters of the molecule of the trimethine cyanine were obtained by DFT method of Gaussian 03." @default.
- W2359954068 created "2016-06-24" @default.
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- W2359954068 date "2008-01-01" @default.
- W2359954068 modified "2023-09-28" @default.
- W2359954068 title "Syntheses and properties of photostable near-infrared cyanines and their cyclodextrin conjugates" @default.
- W2359954068 hasPublicationYear "2008" @default.
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